Evidence map›Paper›PMID 32673397›Full record

ArticleThe Journal of cell biology2020

Intersection of TKS5 and FGD1/CDC42 signaling cascades directs the formation of invadopodia.

Anna Zagryazhskaya-Masson, Pedro Monteiro, Anne-Sophie Macé, Alessia Castagnino, Robin Ferrari, Elvira Infante, Aléria Duperray-Susini, Florent Dingli, Arpad Lanyi, Damarys Loew and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  5. The Duality of Collagens in Metastases of Solid Tumors.International journal of molecular sciences · 2025
    Review
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  16. Genetics of common cerebral small vessel disease.Nature reviews. Neurology · 2022
    Review
  17. Frontiers in pediatrics · 2022
    Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Anna Zagryazhskaya-MassonInstitut Curie, PSL Research University, Centre National de la Recherche Scientifique, UMR 144, Paris, France.
Pedro MonteiroInstitut Curie, PSL Research University, Centre National de la Recherche Scientifique, UMR 144, Paris, France.
Anne-Sophie MacéInstitut Curie, PSL Research University, Centre National de la Recherche Scientifique, UMR 144, Paris, France.
Alessia CastagninoInstitut Curie, PSL Research University, Centre National de la Recherche Scientifique, UMR 144, Paris, France.
Robin FerrariInstitut Curie, PSL Research University, Centre National de la Recherche Scientifique, UMR 144, Paris, France.
Elvira InfanteInstitut Curie, PSL Research University, Centre National de la Recherche Scientifique, UMR 144, Paris, France.
Aléria Duperray-SusiniInstitut Curie, PSL Research University, Centre National de la Recherche Scientifique, UMR 144, Paris, France.
Florent DingliMass Spectrometry and Proteomic Laboratory, Institut Curie, PSL Research University, Paris, France.
Arpad LanyiDepartment of Immunology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Damarys LoewMass Spectrometry and Proteomic Laboratory, Institut Curie, PSL Research University, Paris, France.
Elisabeth GénotEuropean Institute of Chemistry and Biology, Bordeaux, France.
Philippe ChavrierInstitut Curie, PSL Research University, Centre National de la Recherche Scientifique, UMR 144, Paris, France.
Université Paris Sciences et Lettres · FRUniversité de Bordeaux · FRUniversity of Debrecen · HU

Funding

Worldwide Cancer Research 16-1235
6 · The paper itself

Abstract

Tumor cells exposed to a physiological matrix of type I collagen fibers form elongated collagenolytic invadopodia, which differ from dotty-like invadopodia forming on the gelatin substratum model. The related scaffold proteins, TKS5 and TKS4, are key components of the mechanism of invadopodia assembly. The molecular events through which TKS proteins direct collagenolytic invadopodia formation are poorly defined. Using coimmunoprecipitation experiments, identification of bound proteins by mass spectrometry, and in vitro pull-down experiments, we found an interaction between TKS5 and FGD1, a guanine nucleotide exchange factor for the Rho-GTPase CDC42, which is known for its role in the assembly of invadopodial actin core structure. A novel cell polarity network is uncovered comprising TKS5, FGD1, and CDC42, directing invadopodia formation and the polarization of MT1-MMP recycling compartments, required for invadopodia activity and invasion in a 3D collagen matrix. Additionally, our data unveil distinct signaling pathways involved in collagenolytic invadopodia formation downstream of TKS4 or TKS5 in breast cancer cells.

Indexed as

ActinsAdaptor Proteins, Vesicular TransportBreast Neoplasmscdc42 GTP-Binding ProteinCell Line, TumorCell PolarityCollagenFemaleGuanine Nucleotide Exchange FactorsHumansPodosomesrho GTP-Binding ProteinsSignal TransductionTransfectionActinsAdaptor Proteins, Vesicular Transportcdc42 GTP-Binding ProteinCDC42 protein, humanCollagenFGD1 protein, humanGuanine Nucleotide Exchange Factorsrho GTP-Binding ProteinsSH3PXD2A protein, human

Identifiers

PMID32673397
PMCPMC7480108
OpenAlexW3042895833

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.